Face Cancer, Hepatocellular Carcinoma
Conditions
Keywords
TACE, Sorafenib, overall survival, time to progression
Brief summary
Hepatocellular carcinoma (HCC) is the 6th most common cancer and the third most frequent cause of cancer death worldwide. Hepatic resection (HR) has been the standard treatment modality for HCC aiming at clinical cure. In both Europe and Unit States proposed guidelines for HCC, HR was recommend only for patients with a single HCC lesion and preserved liver function . Unfortunately, only 10%-30% of HCCs are amenable to such curative surgical resection at the time of diagnosis, because of tumor multifocality, portal vein invasion, and underlying advanced liver cirrhosis . Alternatively, transarterial chemoembolization (TACE) has become the most popular modality for palliative treatment for the other patients. However, the long term outcomes were generally poor for HCC patients treated with TACE. Recently, sorafenib has shown some promises in improvement of 3-month survival among patients with advanced HCC. It is claimed that sorafenib has become the standard of care for patients advanced HCC. Thus, the purpose of this study was to prospectively compare the effectiveness of sorafenib combined with TACE with that of TACE alone in the treatment of unresectable HCC .
Detailed description
Hepatocellular carcinoma (HCC) is a common cause of cancer mortality in Asia. Most patients present with intermediate or advanced disease. Percutaneous ethanol injection, radiofrequency ablation, and transcatheter arterial chemoembolization (TACE) are not considered as a curative treatment and have achieved very limited success in eradicating large HCC. Two phase III trials were shown to be efficacious and well-tolerated in patients with advanced HCC. Median overall survival was significantly 2 to 3 months longer in the sorafenib group than that in the placebo. It is interesting to recognize the combined therapeutic effect of TACE with sorafenib. The proposed study will make an important contribution to understanding not only the safety and efficacy of sorafenib in addition to TACE in patients diagnosed with unresectable HCC, but this will also be the first clinical trial prospectively to compare the effectiveness of sorafenib combined with TACE with that of TACE alone in the treatment of unresectable HCC
Interventions
PROCEDURETACE-Sorafenib group
Transcatheter arterial chemoembolization drugs and dosage:TACE with chemothrapy drugs (E-ADM 50mg, carboplatin 300 mg, MMC 8mg)and followed with embolization with lipiodol and absorbable gelatin sponge particles or polyvinyl alcohol particles. Oral sorafenib (400 mg BID) will be start the 2-4 weeks after the first TACE treatment and will continue until the patient shows disease progression, until unacceptable toxicity occurs, or until study termination.
PROCEDURETACE
Sponsors
Sun Yat-sen University
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
Only the radiologists who assessed the outcomes were blinded.
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Adults patients ( 18-75 years of age) with a diagnosis of HCC which is not amenable to surgical resection or local ablative therapy 2. Histological confirmed HCC or clinical/laboratory diagnosis of HCC or nodules larger than 2 cm with typical vascular features or AFP \> 200 3. Patient must have quantifiable disease limited to the liver 4. Patients must have at least one tumor lesion that meets both of the following criteria: 5. The lesion can be accurately measured in at least one dimension according to RECIST criteria 6. The lesion has not been previously treated with surgery, radiation therapy, radiofrequency ablation, percutaneous ethanol or acetic acid injection, or cryoablation. 7. ECOG performance status (PS) \<2 8. No prior targeted antiangiogenic therapy. Metronomic chemotherapies are allowed. At least 4 weeks since prior systemic chemotherapy,At least 4 weeks since prior TACE, At least 4 weeks since prior interferon. 9. Not pregnant 10. No significant baseline liver dysfunction. Cirrhotic status of Child-Pugh class A only 11. No significant renal impairment (creatinine clearance \< 30 mL/minute) or patients on dialysis 12. No current infections requiring antibiotic therapy 13. Not on anticoagulation or suffering from a known bleeding disorder 14. No unstable coronary artery disease or recent MI
Exclusion criteria
1. Previous or concurrent cancer that is distinct in primary site or histology from HCC except cervical carcinoma in situ, treated basal-cell carcinoma of the skin, superficial bladder tumors (Ta, Tis & T1), and any cancer curatively treated \> 3 years prior to entry is permitted 2. Renal failure requiring hemo- or peritoneal dialysis 3. Child-Pugh B & C hepatic impairment 4. History of cardiac disease: \> NY Heart Association (NYHA) class 2 congestive heart failure, active coronary artery disease, cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers or digoxin, and uncontrolled hypertension. Myocardial infarction more than 6 months prior to study entry is permitted. 5. Active clinically serious infections (\> CTCAEv3 grade 2) 6. Known history of HIV 7. Known central nervous system tumors including metastatic brain disease 8. History of organ allograft 9. Substance abuse (current), psychological, or social conditions that may interfere with the patient's participation in the study or evaluation of the study results. 10. Known or suspected allergy to the investigational agents or any agent given in association with this trial. 11. Patients unable to swallow oral medications. 12. Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test performed within seven days prior to the start of the study drug. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial. 13. Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy 14. Uncontrolled hypertension defined as systolic blood pressure \> 150 mmHg or diastolic blood pressure \> 90 mmHg, despite optimal medical management 15. Thrombolic or embolic events such as a cerebrovascular accident including transient ischemic attacks within the past 6 months 16. Pulmonary hemorrhage/bleeding event \> CTCAE Grade 2 within 4 weeks of first dose of study drug 17. Any other hemorrhage/bleeding event \> CTCAE Grade 3 within 4 weeks of first dose of study drug 18. Serious non-healing wound, ulcer, or bone fracture
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Effectiveness of sorafenib combined with TACE | 1 year | Measure:overall survival Measured from the date of TACE until the date of death or last visit |
Secondary
| Measure | Time frame |
|---|---|
| Time to progression | 1 year |
Countries
China
Outcome results
None listed